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肾上腺素提高院外心脏骤停患者的生存率:PARAMEDIC2 RCT 研究。

Adrenaline to improve survival in out-of-hospital cardiac arrest: the PARAMEDIC2 RCT.

机构信息

Warwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, UK.

Heartlands Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

出版信息

Health Technol Assess. 2021 Apr;25(25):1-166. doi: 10.3310/hta25250.

Abstract

BACKGROUND

Adrenaline has been used as a treatment for cardiac arrest for many years, despite uncertainty about its effects on long-term outcomes and concerns that it may cause worse neurological outcomes.

OBJECTIVES

The objectives were to evaluate the effects of adrenaline on survival and neurological outcomes, and to assess the cost-effectiveness of adrenaline use.

DESIGN

This was a pragmatic, randomised, allocation-concealed, placebo-controlled, parallel-group superiority trial and economic evaluation. Costs are expressed in Great British pounds and reported in 2016/17 prices.

SETTING

This trial was set in five NHS ambulance services in England and Wales.

PARTICIPANTS

Adults treated for an out-of-hospital cardiac arrest were included. Patients were ineligible if they were pregnant, if they were aged < 16 years, if the cardiac arrest had been caused by anaphylaxis or life-threatening asthma, or if adrenaline had already been given.

INTERVENTIONS

Participants were randomised to either adrenaline (1 mg) or placebo in a 1 : 1 allocation ratio by the opening of allocation-concealed treatment packs.

MAIN OUTCOME MEASURES

The primary outcome was survival to 30 days. The secondary outcomes were survival to hospital admission, survival to hospital discharge, survival at 3, 6 and 12 months, neurological outcomes and health-related quality of life through to 6 months. The economic evaluation assessed the incremental cost per quality-adjusted life-year gained from the perspective of the NHS and Personal Social Services. Participants, clinical teams and those assessing patient outcomes were masked to the treatment allocation.

RESULTS

From December 2014 to October 2017, 8014 participants were assigned to the adrenaline ( = 4015) or to the placebo ( = 3999) arm. At 30 days, 130 out of 4012 participants (3.2%) in the adrenaline arm and 94 out of 3995 (2.4%) in the placebo arm were alive (adjusted odds ratio for survival 1.47, 95% confidence interval 1.09 to 1.97). For secondary outcomes, survival to hospital admission was higher for those receiving adrenaline than for those receiving placebo (23.6% vs. 8.0%; adjusted odds ratio 3.83, 95% confidence interval 3.30 to 4.43). The rate of favourable neurological outcome at hospital discharge was not significantly different between the arms (2.2% vs. 1.9%; adjusted odds ratio 1.19, 95% confidence interval 0.85 to 1.68). The pattern of improved survival but no significant improvement in neurological outcomes continued through to 6 months. By 12 months, survival in the adrenaline arm was 2.7%, compared with 2.0% in the placebo arm (adjusted odds ratio 1.38, 95% confidence interval 1.00 to 1.92). An adjusted subgroup analysis did not identify significant interactions. The incremental cost-effectiveness ratio for adrenaline was estimated at £1,693,003 per quality-adjusted life-year gained over the first 6 months after the cardiac arrest event and £81,070 per quality-adjusted life-year gained over the lifetime of survivors. Additional economic analyses estimated incremental cost-effectiveness ratios for adrenaline at £982,880 per percentage point increase in overall survival and £377,232 per percentage point increase in neurological outcomes over the first 6 months after the cardiac arrest.

LIMITATIONS

The estimate for survival with a favourable neurological outcome is imprecise because of the small numbers of patients surviving with a good outcome.

CONCLUSIONS

Adrenaline improved long-term survival, but there was no evidence that it significantly improved neurological outcomes. The incremental cost-effectiveness ratio per quality-adjusted life-year exceeds the threshold of £20,000-30,000 per quality-adjusted life-year usually supported by the NHS.

FUTURE WORK

Further research is required to better understand patients' preferences in relation to survival and neurological outcomes after out-of-hospital cardiac arrest and to aid interpretation of the trial findings from a patient and public perspective.

TRIAL REGISTRATION

Current Controlled Trials ISRCTN73485024 and EudraCT 2014-000792-11.

FUNDING

This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in ; Vol. 25, No. 25. See the NIHR Journals Library website for further project information.

摘要

背景

尽管肾上腺素对长期预后的影响存在不确定性,并且担心它可能导致更差的神经学结果,但肾上腺素已被多年用于心脏骤停的治疗。

目的

评估肾上腺素对生存率和神经学结果的影响,并评估肾上腺素使用的成本效益。

设计

这是一项实用的、随机的、分配隐藏的、安慰剂对照的、平行组优势试验和经济评估。成本以大不列颠英镑表示,并以 2016/17 年的价格报告。

地点

这项试验在英格兰和威尔士的五个 NH S 救护服务机构进行。

参与者

纳入了因院外心脏骤停而接受治疗的成年人。如果患者怀孕、年龄<16 岁、心脏骤停是由过敏或危及生命的哮喘引起的,或者已经给予肾上腺素,则患者不符合入选条件。

干预措施

通过打开分配隐藏的治疗包,以 1:1 的比例将参与者随机分配至肾上腺素(1mg)或安慰剂组。

主要结局指标

主要结局是 30 天的生存率。次要结局是住院生存率、出院生存率、3、6 和 12 个月的生存率、神经学结局和 6 个月时的健康相关生活质量。经济评估从 NH S 和个人社会服务的角度评估了每获得一个质量调整生命年的增量成本。参与者、临床团队和评估患者结局的人员对治疗分配进行了盲法。

结果

从 2014 年 12 月至 2017 年 10 月,8014 名参与者被分配至肾上腺素(n=4015)或安慰剂(n=3999)组。在 30 天时,肾上腺素组有 4012 名参与者中的 130 名(3.2%)和安慰剂组有 3995 名参与者中的 94 名(2.4%)存活(调整后的生存率比值为 1.47,95%置信区间为 1.09 至 1.97)。对于次要结局,接受肾上腺素治疗的患者住院生存率高于接受安慰剂治疗的患者(23.6% vs. 8.0%;调整后的生存率比值为 3.83,95%置信区间为 3.30 至 4.43)。出院时神经学结局良好的比例在两组之间没有显著差异(2.2% vs. 1.9%;调整后的生存率比值为 1.19,95%置信区间为 0.85 至 1.68)。通过 6 个月的随访,生存率提高但神经学结局没有显著改善的模式仍在继续。在 12 个月时,肾上腺素组的生存率为 2.7%,而安慰剂组为 2.0%(调整后的生存率比值为 1.38,95%置信区间为 1.00 至 1.92)。调整后的亚组分析未发现显著的交互作用。肾上腺素的增量成本效益比估计为每获得 6 个月后第一个 6 个月的质量调整生命年增加 1693003 英镑,幸存者一生中每获得 1 个质量调整生命年增加 81070 英镑。额外的经济分析估计,肾上腺素每增加 6 个月后的总体生存率提高 1 个百分点,以及神经学结局提高 1 个百分点,其增量成本效益比分别为 982880 英镑和 377232 英镑。

局限性

由于存活且结局良好的患者人数较少,因此具有良好神经学结局的生存率的估计结果并不精确。

结论

肾上腺素提高了长期生存率,但没有证据表明它显著改善了神经学结局。每获得 1 个质量调整生命年的增量成本效益比超过了 NH S 通常支持的 20000-30000 英镑/质量调整生命年的阈值。

未来工作

需要进一步研究,以更好地了解院外心脏骤停后患者对生存率和神经学结局的偏好,并从患者和公众的角度帮助解释试验结果。

试验注册

当前对照试验 ISRCTN8443533 和 EudraCT 2014-000792-11。

资金

该项目由英国国立卫生研究院(NIHR)卫生技术评估计划资助,将在;第 25 卷,第 25 期。有关该项目的更多信息,请访问 NIHR 期刊库网站。

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